Development, manufacturing and regulatory from a single source

INOPREX develops, manufactures and takes on regulatory responsibility — in the role that fits your project. For medical devices we act as the legal manufacturer under EU MDR. For cosmetics and food supplements we either take on the role of the responsible person or the person placing the product on the market, or we manage development and production while your brand remains the market operator. Production runs together with leading contract manufacturers and fillers in the EU. Development and regulatory are based in Germany.

Why INOPREX

• Regulatory responsibility from a single source: one contractual partner, one contact.
• Own formulation base for fast white label projects (MOQ from 10,000 units per SKU).
• Experience across all three product categories: medical devices, cosmetics, food supplements.
• Production network in the EU, selected by dosage form, capacity and certification.
• Short decision paths between management, science and production.

Team

• [PLATZHALTER: Foto [PLATZHALTER: Name der Geschäftsführung]]

  [PLATZHALTER: Name der Geschäftsführung]

  Managing Director

  Commercial management, product strategy, international sourcing and market access.

  [PLATZHALTER: LinkedIn-Profil]

• [PLATZHALTER: Foto [PLATZHALTER: Name]]

  [PLATZHALTER: Name]

  Head of Scientific & Technical Affairs

  PhD biochemist with more than ten years of experience in EU MDR, ISO 13485, technical documentation, audit preparation and cooperation with notified bodies.

  [PLATZHALTER: LinkedIn-Profil]

[PLACEHOLDER: further team members, photos and full CVs to be added.]

Location and partner structure

Registered office and development: Teltow near Potsdam (Brandenburg). Production via qualified partners in the EU.